Evidence map›Paper›PMID 28202059›Full record

ArticleStem cell research & therapy2017

Cardiosphere-derived cells do not improve cardiac function in rats with cardiac failure.

Taís Hanae Kasai-Brunswick, Andréa Rodrigues da Costa, Raiana Andrade Quintanilha Barbosa, Bruna Farjun, Fernanda Cristina Paccola Mesquita, Danúbia Silva Dos Santos, Isalira Peroba Ramos, Grazielle Suhett, Guilherme Visconde Brasil, Sandro Torrentes da Cunha and 4 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
4.0field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Utilization of Stem Cells in Medicine: A Narrative Review.International journal of molecular sciences · 2025
    Review
  4. Article
  5. Review
  6. Cell Therapy in the Treatment of Coronary Heart Disease.International journal of molecular sciences · 2023
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 1 country.

Taís Hanae Kasai-BrunswickInstitute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, n°373, room G2-053, CEP:21941-902, Rio de Janeiro, RJ, Brazil.
Andréa Rodrigues da CostaNational Institute of Cardiology, Rua das Laranjeiras, n°374-Laranjeiras, CEP:22240-006, Rio de Janeiro, RJ, Brazil.
Raiana Andrade Quintanilha BarbosaInstitute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, n°373, room G2-053, CEP:21941-902, Rio de Janeiro, RJ, Brazil.
Bruna FarjunInstitute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, n°373, room G2-053, CEP:21941-902, Rio de Janeiro, RJ, Brazil.
Fernanda Cristina Paccola MesquitaInstitute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, n°373, room G2-053, CEP:21941-902, Rio de Janeiro, RJ, Brazil.
Danúbia Silva Dos SantosInstitute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, n°373, room G2-053, CEP:21941-902, Rio de Janeiro, RJ, Brazil.
Isalira Peroba RamosInstitute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, n°373, room G2-053, CEP:21941-902, Rio de Janeiro, RJ, Brazil.
Grazielle SuhettInstitute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, n°373, room G2-053, CEP:21941-902, Rio de Janeiro, RJ, Brazil.
Guilherme Visconde BrasilInstitute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, n°373, room G2-053, CEP:21941-902, Rio de Janeiro, RJ, Brazil.
Sandro Torrentes da CunhaInstitute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, n°373, room G2-053, CEP:21941-902, Rio de Janeiro, RJ, Brazil.
José Oscar R BritoNational Institute of Cardiology, Rua das Laranjeiras, n°374-Laranjeiras, CEP:22240-006, Rio de Janeiro, RJ, Brazil.
Juliana do Amaral PassipieriInstitute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, n°373, room G2-053, CEP:21941-902, Rio de Janeiro, RJ, Brazil.
Adriana Bastos CarvalhoInstitute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, n°373, room G2-053, CEP:21941-902, Rio de Janeiro, RJ, Brazil.
Antonio Carlos Campos de CarvalhoInstitute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, n°373, room G2-053, CEP:21941-902, Rio de Janeiro, RJ, Brazil. acarlos@biof.ufrj.br.
Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro · BRUniversidade Federal do Rio de Janeiro · BRInstituto Nacional de Cardiologia · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHeart failure represents an important public health issue due to its high costs and growing incidence worldwide. Evidence showing the regenerative potential of postmitotic heart tissue has suggested the existence of endogenous cardiac stem cells in adult hearts. Cardiosphere-derived cells (CDC) constitute a candidate pool of such cardiac stem cells. Previous studies using acute myocardial infarction (MI) models in rodents demonstrated an improvement in cardiac function after cell therapy with CDC. We evaluated the therapeutic potential of CDC 60 days after MI in a rat model.

methodsCDC were obtained from human discarded myocardial tissue and rat hearts by enzymatic digestion with collagenase II. At 10-15 days after isolation, small, round, phase-bright cells (PBCs) appeared on top of the adherent fibroblast-like cells. The PBCs were collected and placed on a nonadherent plate for 2 days, where they formed cardiospheres which were then transferred to adherent plates, giving rise to CDC. These CDC were characterized by flow cytometry. Wistar rats were submitted to MI through permanent occlusion of the anterior descending coronary artery. After 60 days, they were immunosuppressed with cyclosporine A during 10 days. On the third day, infarcted animals were treated with 5 × 10

resultsCDC had a predominantly mesenchymal phenotype. Cell tracking by bioluminescence demonstrated over 85% decrease in signal at 5-7 days after cell therapy. Cardiac function evaluation by echocardiography showed no differences in ejection fraction, end-diastolic volume, or end-systolic volume between groups receiving human cells, rat cells, or placebo. Hemodynamic analyses and infarct area quantification confirmed that there was no improvement in cardiac remodeling after cell therapy with CDC.

conclusionOur study challenges the effectiveness of CDC in post-ischemic heart failure.

Indexed as

Immunocompromised HostAnimalsCoronary OcclusionCoronary VesselsCyclosporineDisease Models, AnimalEchocardiographyHeart Function TestsHumansInjections, IntralesionalMyocardial InfarctionRatsRats, WistarSpheroids, CellularStem CellsTreatment FailureCyclosporineBioluminescenceCardiosphere-derived cellsCell therapyHeart failureMyocardial infarctionStem cells

Identifiers

PMID28202059
PMCPMC5312520
OpenAlexW2588560226

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.